Fusarium solani
Fusarium solani is listed in the FDA National Drug Code directory with 5 NDC codes, marketed under brand names including Fusarium solani, Fusarium. Available dosage forms: solution, injection.
Drug Details
- Generic Name
- Fusarium solani
- Brand Names
- Fusarium solani, Fusarium
- Application Number
- BLA101833
- Sponsor
- Greer Laboratories, Inc.
- NDC Codes
- 5
- Dosage Forms
- SOLUTION, INJECTION
- Routes
- INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS, CUTANEOUS
- Active Ingredients
- HAEMATONECTRIA HAEMATOCOCCA
Indications and Usage
USES: May help temporarily relieve allergy symptoms ■ headache ■ itchy, watery eyes ■ sneezing* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Warnings
WARNINGS: Stop use and ask a doctor if ■ symptoms do not improve in 5 days or new symptoms appear ■ you are an asthma sufferer with severe mold allergies If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if printed foil blister is broken or missing. ■ Store at room temperature (65-80ºF)